tyrosine has been researched along with Albers-Schoenberg Disease in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ahariz, N; Cambisano, N; Charlier, C; Coppieters, W; Druet, T; Fasquelle, C; Jentsch, TJ; Ludwig, CF; Sartelet, A; Stauber, T; Zhang, Z | 1 |
Liu, J; Pei, D; Shu, X; Wang, Q; Xu, J; Xu, T; Ye, Y | 1 |
Groth, CG; Ringdén, O | 1 |
Francis, MJ; Macmillan, DC; Smith, R | 1 |
1 review(s) available for tyrosine and Albers-Schoenberg Disease
Article | Year |
---|---|
Transplantation in relation to the treatment of inherited disease.
Topics: alpha 1-Antitrypsin Deficiency; Amyloidosis; Bone Marrow Transplantation; Fabry Disease; Gaucher Disease; Genetic Diseases, Inborn; Gout; Granulomatous Disease, Chronic; Hemoglobinopathies; Hemophilia A; Hepatolenticular Degeneration; Humans; Immunologic Deficiency Syndromes; Kidney Transplantation; Leukodystrophy, Metachromatic; Liver Transplantation; Lymphocytes; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nephritis, Hereditary; Niemann-Pick Diseases; Osteopetrosis; Oxalates; Oxalic Acid; Transplantation; Tyrosine; Uremia | 1984 |
3 other study(ies) available for tyrosine and Albers-Schoenberg Disease
Article | Year |
---|---|
A missense mutation accelerating the gating of the lysosomal Cl-/H+-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle.
Topics: Amino Acid Sequence; Animals; Cattle; Chloride Channels; Genome-Wide Association Study; Genotype; Gingival Diseases; Hamartoma; Haplotypes; HeLa Cells; Homeostasis; Homozygote; Humans; Lysosomes; Membrane Proteins; Mice; Molecular Sequence Data; Mutation, Missense; Osteopetrosis; Sequence Homology, Amino Acid; Tyrosine; Ubiquitin-Protein Ligases; Xenopus laevis | 2014 |
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis.
Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Humans; MCF-7 Cells; Models, Molecular; Molecular Sequence Data; Mutation; Osteoclasts; Osteopetrosis; Protein Conformation; Protein Interaction Domains and Motifs; Protein Stability; Protein Structure, Tertiary; Protein Transport; Recombinant Proteins; Sequence Alignment; Sorting Nexins; Tyrosine; Vacuoles | 2014 |
Polymeric collagen of skin in normal sunjects and in patients with inherited connective tissue disorders.
Topics: Acromegaly; Adolescent; Adult; Aged; Child; Child, Preschool; Collagen; Collagen Diseases; Female; Hexosamines; Homocystinuria; Hot Temperature; Humans; Hyperparathyroidism; Male; Microscopy, Electron; Middle Aged; Myositis Ossificans; Osteitis Deformans; Osteogenesis Imperfecta; Osteopetrosis; Pseudoxanthoma Elasticum; Skin; Tyrosine; Werner Syndrome | 1973 |